Abstract
Sickle cell disease (SCD) is a hereditary blood disorder affecting the shape of the red blood cells that block blood vessels leading to organ damage and frequent erratic painful episodes. SCD is a global public health issue affecting millions of people throughout the world. This article explores (a) what SCD is; (b) the physical and psychosocial impacts of the disease; (c) the challenges and opportunities associated with sickle cell prevention, education, and management; and (d) the implications for social work policy, practice, and research associated with the identified challenges and opportunities.
Notes
1. Individuals with SCT are usually healthy with no symptoms; however, they can transmit the SCT to their offspring (Centers for Disease Control and Prevention, Citation2011).
2. Vasoocclusion occurs when the sickled red blood cells (RBC) obstruct the other blood cells resulting in an inadequate supply of blood to the organs (Creary et al., Citation2007).
3. Complete or partial collapse of the lung.